# FDA recall Z-1452-2022

> **Stryker Instruments Div. of Stryker Corporation** · Class II · device recall initiated 2022-06-15.

## Product

SurgiCount+ System Application, Software Version 2.0.17, Catalog Number 0694-002-090.  Used for counting, displaying, recording and locating the number of RFID-tagged absorbent articles used during surgical procedures.

## Reason for recall

When scanning sponges out after a surgical procedure, an error may allow for a duplicate sponge to be counted without the prompt to make a case note and allowing the case to close. The software update will prevent the occurrence of this error.

## Distribution

The products were distributed to the following US states: KS and ME.

## Key facts

- **Recall number:** Z-1452-2022
- **Recalling firm:** Stryker Instruments Div. of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-06-15
- **Report date:** 2022-07-27
- **Termination date:** 2024-04-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1452-2022

## Citation

> AI Analytics. FDA recall Z-1452-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1452-2022. Source: US FDA. Licensed CC0.

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